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Wide phenotypic spectrum of the TARDBP gene: homozygosity of A382T mutation in a patient presenting with amyotrophic lateral sclerosis, Parkinson's disease, and frontotemporal lobar degeneration, and in neurologically healthy subject
Lorena Mosca, Christian Lunetta, Claudia Tarlarini, Francesca Avemaria, Eleonora Maestri, Mario Melazzini, Massimo Corbo, Silvana PencoVolume:
33
Year:
2012
Language:
english
DOI:
10.1016/j.neurobiolaging.2012.01.108
File:
PDF, 418 KB
english, 2012